Technology Process of (1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-3a-aminium chloride
There total 7 articles about (1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-(prop-1-en-2-yl)icosahydro-1H-cyclopenta[a]chrysen-3a-aminium chloride which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
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628308-21-4
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-isocyanato-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)octadecahydro-1H-cyclopenta[a]chrysen-9(5bH)-one
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1449661-53-3
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-amino-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)octadecahydro-1H-cyclopenta[a]chrysen-9(5bH)-one hydrochloride
- Guidance literature:
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With
hydrogenchloride; water;
In
1,4-dioxane;
at 20 ℃;
for 6h;
Concentration;
Temperature;
Time;
Inert atmosphere;
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1449661-53-3
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-amino-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)octadecahydro-1H-cyclopenta[a]chrysen-9(5bH)-one hydrochloride
- Guidance literature:
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Multi-step reaction with 3 steps
1: triethylamine; diphenyl phosphoryl azide / 1,4-dioxane / 26 h / Inert atmosphere; Reflux
2: pyridinium chlorochromate / dichloromethane / 6.75 h / 20 °C / Inert atmosphere
3: hydrogenchloride; water / 1,4-dioxane / 6 h / 20 °C / Inert atmosphere
With
hydrogenchloride; diphenyl phosphoryl azide; water; triethylamine; pyridinium chlorochromate;
In
1,4-dioxane; dichloromethane;
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1449661-53-3
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-amino-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)octadecahydro-1H-cyclopenta[a]chrysen-9(5bH)-one hydrochloride
- Guidance literature:
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Multi-step reaction with 4 steps
1: 4-methylmorpholine N-oxide; tetrapropylammonium perruthennate / dichloromethane; acetonitrile / 20 °C / Inert atmosphere; Molecular sieve
2: 2-methyl-but-2-ene; sodium chlorite; sodium dihydrogen phosphate monohydrate / water; tert-butyl alcohol / 2 h / 20 °C / Inert atmosphere
3: diphenyl phosphoryl azide; N-ethyl-N,N-diisopropylamine / 1,4-dioxane / 16.66 h / 20 - 102 °C / Inert atmosphere
4: hydrogenchloride; water / 1,4-dioxane / 6 h / 20 °C / Inert atmosphere
With
hydrogenchloride; sodium chlorite; tetrapropylammonium perruthennate; sodium dihydrogen phosphate monohydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; water; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine;
In
1,4-dioxane; dichloromethane; water; acetonitrile; tert-butyl alcohol;